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rs876661130

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661130(A;A)
Make rs876661130(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position89984556
GeneNBN
is asnp
is mentioned by
dbSNPrs876661130
ebirs876661130
HLIrs876661130
Exacrs876661130
Varsomers876661130
Maprs876661130
PheGenIrs876661130
hapmaprs876661130
1000 genomesrs876661130
hgdprs876661130
ensemblrs876661130
gopubmedrs876661130
geneviewrs876661130
scholarrs876661130
googlers876661130
pharmgkbrs876661130
gwascentralrs876661130
openSNPrs876661130
23andMers876661130
23andMe allrs876661130
SNP Nexus

SNPshotrs876661130
SNPdbers876661130
MSV3drs876661130
GWAS Ctlgrs876661130
Max Magnitude0
ClinVar
Risk rs876661130(A;A)
Alt rs876661130(A;A)
Reference rs876661130(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NBN
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.90996784C>T
CLNSRC
CLNACC RCV000220864.1,